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	Title	Author(s)	Issue Date
	MR imaging of spinal tumors in children with neurofibromatosis I Journal:American Journal of Roentgenology	Khong, PL Goh, WHS Wong, VCN Fung, CW Ooi, GC	2003
	NDUFA9 point mutations cause a variable mitochondrial complex I assembly defect Journal:Clinical Genetics	Baertling, F Sánche-Caballero, L van den Brand, MAM Fung, CW Chan, HSS Wong, CNV Hellebrekers, DME de Coo, IFM Smeitink, JAN AM Rodnburg, RJT Nijtmans, LGJ	2018
	Neuromuscular involvement in children with mitochondrial disease: A single centre experience Proceeding/Conference:14th Asian and Oceanian Congress of Child Neurology	Chiu, ATG Fung, CW Chan, HSS	2017
	Novel POLG mutation in a patient with sensory ataxia, neuropathy, ophthalmoparesis and stroke Journal:Clinica Chimica Acta	Lam, CW Law, CY Siu, CWK Fung, CW Yau, MM Huen, KF Lee, HHC Mak, CM	2015
	Partnering role of FOXM1 and EPS8 in maintaining chemoresistance in human ovarian cancer Proceeding/Conference:Hong Kong Inter-University Postgraduate Symposium in Biochemical Sciences, 2017	Fung, CW Chan, DW Yao, KM	2017
	A rare cause of hepatosplenomegaly - transaldolase deficiency Proceeding/Conference:Annual Symposium of Society for the Study of Inborn Errors of Metabolism, SSIEM 2007	Fung, CW Siu, S Mak, C Poon, GWK Cheung, PT Low, LCK Tam, S Wong, VCN	2007
	A rare cause of hepatosplenomegaly transaldolase deficiency Proceeding/Conference:Joint Annual Scientific Meeting for Paediatricians & Paediatric Nurses	Fung, CW Siu, S Mak, CM Poon, GWK Wong, KY Cheung, PT Low, LCK Tam, S Wong, VCN	2007
	Spectrum of mitochondrial diseases in a tertiary referral centre in Hong Kong Proceeding/Conference:International Symposium on Epilepsy in Neurometabolic Diseases, ISENMD 2010 Proceedings	Fung, CW Poon, G Kwok, A Cheung, PT Low, L Mak, C Tam, S Siu, S Wong, V	2010
	A study of cerebrospinal fluid neurotransmitters assay in children with undiagnosed neurological diseases in Hong Kong Proceeding/Conference:International Symposium on Epilepsy in Neurometabolic Diseases, ISENMD 2010 Proceedings	Fung, CW Poon, G Kwok, A Cheung, PT Low, L Blau, N Siu, S Mak, C Tam, S Wong, V	2010
	The KLHL40 c.1516A>C is a Chinese‐specific founder mutation causing nemaline myopathy 8: Report of six patients with pre‐ and postnatal phenotypes Journal:Molecular Genetics & Genomic Medicine	Yeung, KS Yu, FNY Fung, CW Wong, S Lee, HCH Fung, STH Fung, GPG Leung, KY Chung, WH Lee, YT Ng, VKS YU, HC Fung, JLF TSANG, MHY Chan, KYK Chan, SHS Kan, ASY Chung, BHY	2020
	Video-fluoroscopic study of swallowing in children with neurodevelopmental disorders Journal:Pediatrics International	Fung, CW Khong, PL To, R Goh, W Wong, V	2004

Showing results 8 to 18 of 18 < previous